AU698250B2 - Recombinant DNA viral vector for transfecting animal cells - Google Patents
Recombinant DNA viral vector for transfecting animal cells Download PDFInfo
- Publication number
- AU698250B2 AU698250B2 AU30248/95A AU3024895A AU698250B2 AU 698250 B2 AU698250 B2 AU 698250B2 AU 30248/95 A AU30248/95 A AU 30248/95A AU 3024895 A AU3024895 A AU 3024895A AU 698250 B2 AU698250 B2 AU 698250B2
- Authority
- AU
- Australia
- Prior art keywords
- recombinase
- sequence
- replication
- promoter
- gene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 210000004102 animal cell Anatomy 0.000 title claims abstract description 37
- 239000013603 viral vector Substances 0.000 title claims abstract description 15
- 108020004511 Recombinant DNA Proteins 0.000 title claims abstract description 10
- 239000013598 vector Substances 0.000 claims abstract description 99
- 108020004414 DNA Proteins 0.000 claims abstract description 87
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 85
- 230000010076 replication Effects 0.000 claims abstract description 55
- 239000012634 fragment Substances 0.000 claims abstract description 52
- 108010091086 Recombinases Proteins 0.000 claims abstract description 45
- 108091034057 RNA (poly(A)) Proteins 0.000 claims abstract description 36
- 102000018120 Recombinases Human genes 0.000 claims abstract description 29
- 102000053602 DNA Human genes 0.000 claims abstract description 25
- 108020004638 Circular DNA Proteins 0.000 claims abstract description 24
- 238000001415 gene therapy Methods 0.000 claims abstract description 17
- 208000026350 Inborn Genetic disease Diseases 0.000 claims abstract description 4
- 230000009471 action Effects 0.000 claims abstract description 4
- 230000002950 deficient Effects 0.000 claims abstract description 4
- 208000024556 Mendelian disease Diseases 0.000 claims abstract description 3
- 210000004027 cell Anatomy 0.000 claims description 107
- 238000000034 method Methods 0.000 claims description 46
- 241000701161 unidentified adenovirus Species 0.000 claims description 36
- 241000700605 Viruses Species 0.000 claims description 31
- 101710200251 Recombinase cre Proteins 0.000 claims description 21
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 11
- 241000894007 species Species 0.000 claims description 6
- 230000002463 transducing effect Effects 0.000 claims description 6
- 238000011144 upstream manufacturing Methods 0.000 claims description 6
- 238000001890 transfection Methods 0.000 claims description 5
- 241000283973 Oryctolagus cuniculus Species 0.000 claims description 4
- 230000003362 replicative effect Effects 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 241000701022 Cytomegalovirus Species 0.000 claims description 3
- 241000287828 Gallus gallus Species 0.000 claims description 3
- 241000125945 Protoparvovirus Species 0.000 claims description 3
- 239000003623 enhancer Substances 0.000 claims description 3
- 241001529453 unidentified herpesvirus Species 0.000 claims description 3
- 208000028782 Hereditary disease Diseases 0.000 abstract 1
- 239000013612 plasmid Substances 0.000 description 46
- 239000000243 solution Substances 0.000 description 33
- 230000014509 gene expression Effects 0.000 description 30
- 108091008146 restriction endonucleases Proteins 0.000 description 27
- 239000000047 product Substances 0.000 description 23
- 102000004190 Enzymes Human genes 0.000 description 16
- 108090000790 Enzymes Proteins 0.000 description 16
- 238000001962 electrophoresis Methods 0.000 description 16
- 230000003612 virological effect Effects 0.000 description 16
- 239000000203 mixture Substances 0.000 description 13
- 241001465754 Metazoa Species 0.000 description 10
- 241000588724 Escherichia coli Species 0.000 description 9
- 239000002609 medium Substances 0.000 description 9
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 8
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 8
- 239000011543 agarose gel Substances 0.000 description 8
- 238000005119 centrifugation Methods 0.000 description 8
- 230000029087 digestion Effects 0.000 description 8
- 102000039446 nucleic acids Human genes 0.000 description 8
- 108020004707 nucleic acids Proteins 0.000 description 8
- 150000007523 nucleic acids Chemical class 0.000 description 8
- 101100007328 Cocos nucifera COS-1 gene Proteins 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000003752 polymerase chain reaction Methods 0.000 description 7
- 239000006228 supernatant Substances 0.000 description 7
- 102000012410 DNA Ligases Human genes 0.000 description 6
- 108010061982 DNA Ligases Proteins 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 210000004940 nucleus Anatomy 0.000 description 6
- 241001430294 unidentified retrovirus Species 0.000 description 6
- 108091007433 antigens Proteins 0.000 description 5
- 238000010276 construction Methods 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000010361 transduction Methods 0.000 description 5
- 230000026683 transduction Effects 0.000 description 5
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 102000003960 Ligases Human genes 0.000 description 4
- 108090000364 Ligases Proteins 0.000 description 4
- 230000000692 anti-sense effect Effects 0.000 description 4
- 239000000427 antigen Substances 0.000 description 4
- 102000036639 antigens Human genes 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 239000002299 complementary DNA Substances 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 239000001963 growth medium Substances 0.000 description 4
- 210000005260 human cell Anatomy 0.000 description 4
- 238000000338 in vitro Methods 0.000 description 4
- 210000000653 nervous system Anatomy 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 244000195895 saibo Species 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 3
- 102000008186 Collagen Human genes 0.000 description 3
- 108010035532 Collagen Proteins 0.000 description 3
- 241000702191 Escherichia virus P1 Species 0.000 description 3
- 241000700721 Hepatitis B virus Species 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 3
- 229960000723 ampicillin Drugs 0.000 description 3
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 3
- 230000001413 cellular effect Effects 0.000 description 3
- 210000000349 chromosome Anatomy 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- 229920001436 collagen Polymers 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000012217 deletion Methods 0.000 description 3
- 230000037430 deletion Effects 0.000 description 3
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 description 3
- 229960005542 ethidium bromide Drugs 0.000 description 3
- 239000013604 expression vector Substances 0.000 description 3
- 238000002523 gelfiltration Methods 0.000 description 3
- 229960000789 guanidine hydrochloride Drugs 0.000 description 3
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000000644 propagated effect Effects 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 238000010257 thawing Methods 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 238000005199 ultracentrifugation Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 108010067770 Endopeptidase K Proteins 0.000 description 2
- 108010051696 Growth Hormone Proteins 0.000 description 2
- 102000018997 Growth Hormone Human genes 0.000 description 2
- 241000598171 Human adenovirus sp. Species 0.000 description 2
- 102100024640 Low-density lipoprotein receptor Human genes 0.000 description 2
- 239000006142 Luria-Bertani Agar Substances 0.000 description 2
- 108091034117 Oligonucleotide Proteins 0.000 description 2
- 108010076504 Protein Sorting Signals Proteins 0.000 description 2
- 108091081062 Repeated sequence (DNA) Proteins 0.000 description 2
- 238000002105 Southern blotting Methods 0.000 description 2
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 2
- 108700005077 Viral Genes Proteins 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 108091092356 cellular DNA Proteins 0.000 description 2
- 210000004748 cultured cell Anatomy 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 108010030074 endodeoxyribonuclease MluI Proteins 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000012869 ethanol precipitation Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000000122 growth hormone Substances 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000010369 molecular cloning Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000000284 resting effect Effects 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 101710169336 5'-deoxyadenosine deaminase Proteins 0.000 description 1
- 102000055025 Adenosine deaminases Human genes 0.000 description 1
- 101710081722 Antitrypsin Proteins 0.000 description 1
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 description 1
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 102100022641 Coagulation factor IX Human genes 0.000 description 1
- 208000003322 Coinfection Diseases 0.000 description 1
- 206010010144 Completed suicide Diseases 0.000 description 1
- 201000003883 Cystic fibrosis Diseases 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 102000000311 Cytosine Deaminase Human genes 0.000 description 1
- 108010080611 Cytosine Deaminase Proteins 0.000 description 1
- 108010076804 DNA Restriction Enzymes Proteins 0.000 description 1
- 238000012270 DNA recombination Methods 0.000 description 1
- 101100011399 Danio rerio eif3ea gene Proteins 0.000 description 1
- 102000001039 Dystrophin Human genes 0.000 description 1
- 108010069091 Dystrophin Proteins 0.000 description 1
- 101150005585 E3 gene Proteins 0.000 description 1
- 102000003951 Erythropoietin Human genes 0.000 description 1
- 108090000394 Erythropoietin Proteins 0.000 description 1
- 102000008016 Eukaryotic Initiation Factor-3 Human genes 0.000 description 1
- 108010076282 Factor IX Proteins 0.000 description 1
- 108010054218 Factor VIII Proteins 0.000 description 1
- 102000001690 Factor VIII Human genes 0.000 description 1
- 102000002464 Galactosidases Human genes 0.000 description 1
- 108010093031 Galactosidases Proteins 0.000 description 1
- 102000004269 Granulocyte Colony-Stimulating Factor Human genes 0.000 description 1
- 108010017080 Granulocyte Colony-Stimulating Factor Proteins 0.000 description 1
- 102000004457 Granulocyte-Macrophage Colony-Stimulating Factor Human genes 0.000 description 1
- 108010017213 Granulocyte-Macrophage Colony-Stimulating Factor Proteins 0.000 description 1
- 101000979629 Homo sapiens Nucleoside diphosphate kinase A Proteins 0.000 description 1
- 208000000563 Hyperlipoproteinemia Type II Diseases 0.000 description 1
- 101150008815 INT6 gene Proteins 0.000 description 1
- 108700005091 Immunoglobulin Genes Proteins 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 102000015696 Interleukins Human genes 0.000 description 1
- 108010063738 Interleukins Proteins 0.000 description 1
- 108010001831 LDL receptors Proteins 0.000 description 1
- 101710192606 Latent membrane protein 2 Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 108010025020 Nerve Growth Factor Proteins 0.000 description 1
- 102000007072 Nerve Growth Factors Human genes 0.000 description 1
- 102100023252 Nucleoside diphosphate kinase A Human genes 0.000 description 1
- 108700020796 Oncogene Proteins 0.000 description 1
- 101150101654 PSR1 gene Proteins 0.000 description 1
- 101150090155 R gene Proteins 0.000 description 1
- 108020005091 Replication Origin Proteins 0.000 description 1
- 102000006382 Ribonucleases Human genes 0.000 description 1
- 108010083644 Ribonucleases Proteins 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 241000235346 Schizosaccharomyces Species 0.000 description 1
- 101710109576 Terminal protein Proteins 0.000 description 1
- 102000006601 Thymidine Kinase Human genes 0.000 description 1
- 108020004440 Thymidine kinase Proteins 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 108700025716 Tumor Suppressor Genes Proteins 0.000 description 1
- 102000044209 Tumor Suppressor Genes Human genes 0.000 description 1
- 206010054094 Tumour necrosis Diseases 0.000 description 1
- 206010045261 Type IIa hyperlipidaemia Diseases 0.000 description 1
- 108020005202 Viral DNA Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000001475 anti-trypsic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- YTRQFSDWAXHJCC-UHFFFAOYSA-N chloroform;phenol Chemical compound ClC(Cl)Cl.OC1=CC=CC=C1 YTRQFSDWAXHJCC-UHFFFAOYSA-N 0.000 description 1
- 238000012761 co-transfection Methods 0.000 description 1
- 229940105774 coagulation factor ix Drugs 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 101150036876 cre gene Proteins 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002702 enteric coating Substances 0.000 description 1
- 238000009505 enteric coating Methods 0.000 description 1
- 230000006862 enzymatic digestion Effects 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 229940105423 erythropoietin Drugs 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 201000001386 familial hypercholesterolemia Diseases 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 210000002950 fibroblast Anatomy 0.000 description 1
- 101150042777 flp gene Proteins 0.000 description 1
- 238000012757 fluorescence staining Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 208000016361 genetic disease Diseases 0.000 description 1
- 229960004198 guanidine Drugs 0.000 description 1
- -1 guanidine hydrochloridesaturated cesium chloride Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 230000002608 insulinlike Effects 0.000 description 1
- 229940047122 interleukins Drugs 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000001738 isopycnic centrifugation Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000000394 mitotic effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003147 molecular marker Substances 0.000 description 1
- 230000003387 muscular Effects 0.000 description 1
- 201000006938 muscular dystrophy Diseases 0.000 description 1
- 230000010309 neoplastic transformation Effects 0.000 description 1
- 239000003900 neurotrophic factor Substances 0.000 description 1
- 210000003240 portal vein Anatomy 0.000 description 1
- OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000012679 serum free medium Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 229940104230 thymidine Drugs 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 241001515965 unidentified phage Species 0.000 description 1
- 108700026215 vpr Genes Proteins 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
- C12N2710/10343—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2800/00—Nucleic acids vectors
- C12N2800/10—Plasmid DNA
- C12N2800/108—Plasmid DNA episomal vectors
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2800/00—Nucleic acids vectors
- C12N2800/30—Vector systems comprising sequences for excision in presence of a recombinase, e.g. loxP or FRT
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25131294A JP4216350B2 (ja) | 1994-09-19 | 1994-09-19 | 動物細胞感染用の組換えｄｎａウイルスベクター |
| JP6-251312 | 1994-09-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU3024895A AU3024895A (en) | 1996-04-04 |
| AU698250B2 true AU698250B2 (en) | 1998-10-29 |
Family
ID=17220940
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU30248/95A Expired AU698250B2 (en) | 1994-09-19 | 1995-08-25 | Recombinant DNA viral vector for transfecting animal cells |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5817492A (ko) |
| EP (1) | EP0704534B1 (ko) |
| JP (1) | JP4216350B2 (ko) |
| KR (1) | KR100379654B1 (ko) |
| CN (1) | CN1077919C (ko) |
| AT (1) | ATE321874T1 (ko) |
| AU (1) | AU698250B2 (ko) |
| CA (1) | CA2157063C (ko) |
| DE (1) | DE69534902T2 (ko) |
| NZ (1) | NZ272883A (ko) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6120764A (en) * | 1993-06-24 | 2000-09-19 | Advec, Inc. | Adenoviruses for control of gene expression |
| US5919676A (en) * | 1993-06-24 | 1999-07-06 | Advec, Inc. | Adenoviral vector system comprising Cre-loxP recombination |
| US6974694B2 (en) | 1995-06-07 | 2005-12-13 | Advec, Inc. | Adenoviruses for control of gene expression |
| DE19530412A1 (de) * | 1995-08-18 | 1997-02-20 | Harald Von Prof Dr Melchner | Selbst deletierende retrovirale Vektoren für die Gentherapie |
| US5801030A (en) * | 1995-09-01 | 1998-09-01 | Genvec, Inc. | Methods and vectors for site-specific recombination |
| WO1997019181A2 (de) * | 1995-11-24 | 1997-05-29 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Berlin | Virusvektor für den transfer stabiler episome |
| FR2749857B1 (fr) | 1996-06-12 | 1998-08-14 | Centre Nat Rech Scient | Generation de molecules replicatives in vivo |
| EP0932679A1 (en) * | 1996-10-18 | 1999-08-04 | CANJI, Inc. | METHODS AND COMPOSITIONS FOR DELIVERY AND EXPRESSION OF INTERFERON-$g(a) NUCLEIC ACIDS |
| US20030125278A1 (en) * | 1997-08-13 | 2003-07-03 | Tang De-Chu C. | Immunization of animals by topical applications of a salmonella-based vector |
| US6716823B1 (en) | 1997-08-13 | 2004-04-06 | The Uab Research Foundation | Noninvasive genetic immunization, expression products therefrom, and uses thereof |
| US6706693B1 (en) | 1997-08-13 | 2004-03-16 | The Uab Research Foundation | Vaccination by topical application of genetic vectors |
| US20030045492A1 (en) * | 1997-08-13 | 2003-03-06 | Tang De-Chu C. | Vaccination by topical application of recombinant vectors |
| US6348450B1 (en) * | 1997-08-13 | 2002-02-19 | The Uab Research Foundation | Noninvasive genetic immunization, expression products therefrom and uses thereof |
| EP1023442B1 (en) * | 1997-10-16 | 2010-11-24 | University Of Georgia Research Foundation, Inc. | Transgenic birds and protein production |
| US7098191B2 (en) * | 1997-11-03 | 2006-08-29 | The Arizona Board Of Reagents | Hyperthermic inducible expression vectors for gene therapy and methods of use thereof |
| US6709858B1 (en) * | 1997-11-03 | 2004-03-23 | The Arizona Board Of Regents On Behalf Of The University Of Arizona | Hyperthermic inducible expression vectors for gene therapy and methods of use thereof |
| CA2346800A1 (en) * | 1998-10-12 | 2000-04-20 | Sumitomo Pharmaceuticals Company, Limited | Cells expressing recombinase |
| US6395549B1 (en) | 1998-10-22 | 2002-05-28 | Medical College Of Georgia Research Institute, Inc. | Long terminal repeat, enhancer, and insulator sequences for use in recombinant vectors |
| EP1159439B1 (en) * | 1999-03-05 | 2014-01-08 | Advec Inc. | Enhanced system for construction of adenovirus vectors |
| US6890726B1 (en) | 1999-04-06 | 2005-05-10 | Oklahoma Medical Research Foundation | Method for selecting recombinase variants with altered specificity |
| US20040009936A1 (en) * | 1999-05-03 | 2004-01-15 | Tang De-Chu C. | Vaccine and drug delivery by topical application of vectors and vector extracts |
| WO2002006451A1 (en) * | 2000-07-18 | 2002-01-24 | Uab Research Foundation | Tissue-specific self-inactivating gene therapy vector |
| US7198924B2 (en) | 2000-12-11 | 2007-04-03 | Invitrogen Corporation | Methods and compositions for synthesis of nucleic acid molecules using multiple recognition sites |
| CA2442144A1 (en) * | 2001-03-26 | 2002-11-21 | The Board Of Trustees Of The Leland Stanford Junior University | A helper dependent adenoviral vector system and methods for using the same |
| CA2451957A1 (en) * | 2001-06-28 | 2003-01-09 | Phenogene Therapeutiques Inc. | Methods, vectors, cell lines and kits for selecting nucleic acids having a desired feature |
| US7164056B2 (en) * | 2002-05-03 | 2007-01-16 | Pioneer Hi-Bred International, Inc. | Gene targeting using replicating DNA molecules |
| AU2003242380A1 (en) * | 2002-06-17 | 2003-12-31 | Nagoya Industrial Science Research Institute | Method of slective isolation or visualization of target cells differentiated from embryonic stem cells or kit for visualization |
| US20040203133A1 (en) * | 2003-01-07 | 2004-10-14 | Anja Ehrhardt | Helper dependent adenoviral vector system and methods for using the same |
| US20050130919A1 (en) * | 2003-07-18 | 2005-06-16 | University Of Massachusetts | Regulatable promoters for synthesis of small hairpin RNA |
| JP4478775B2 (ja) * | 2003-07-31 | 2010-06-09 | 財団法人名古屋産業科学研究所 | 増殖制御型組換えアデノウイルスベクターの効率的な作製方法及びその作製用キット |
| US20060239966A1 (en) * | 2003-10-20 | 2006-10-26 | Tornoee Jens | In vivo gene therapy of parkinson's disease |
| WO2005054438A2 (en) | 2003-12-01 | 2005-06-16 | Invitrogen Corporation | Nucleic acid molecules containing recombination sites and methods of using the same |
| JP2008531581A (ja) * | 2005-02-23 | 2008-08-14 | ユーエービー リサーチ ファウンデーション | アルキル−グリコシドで増強されたワクチン接種 |
| US20090068158A1 (en) * | 2005-12-09 | 2009-03-12 | Medin Jeffrey A | Thymidylate kinase mutants and uses thereof |
| CA2566267A1 (en) * | 2005-12-09 | 2007-06-09 | University Health Network | Thymidylate kinase mutants and uses thereof |
| EP2502999A3 (en) | 2006-03-03 | 2013-01-23 | Amorfix Life Sciences Ltd. | Methods and compositions to treat and detect misfolded-SOD1 mediated diseases |
| CA2584494A1 (en) * | 2007-03-27 | 2008-09-27 | Jeffrey A. Medin | Vector encoding therapeutic polypeptide and safety elements to clear transduced cells |
| ES2654303T3 (es) | 2007-05-04 | 2018-02-13 | University Health Network | Inmunoterapia de IL-12 contra el cáncer |
| JP2008307007A (ja) | 2007-06-15 | 2008-12-25 | Bayer Schering Pharma Ag | 出生後のヒト組織由来未分化幹細胞から誘導したヒト多能性幹細胞 |
| US8568709B2 (en) | 2008-03-20 | 2013-10-29 | University Health Network | Thymidylate kinase fusions and uses thereof |
| KR101661940B1 (ko) | 2008-05-02 | 2016-10-04 | 고쿠리츠 다이가쿠 호진 교토 다이가쿠 | 핵 초기화 방법 |
| US8629334B2 (en) * | 2008-07-16 | 2014-01-14 | University Of Florida Research Foundation, Inc. | Viral-based transient-expression vector system for trees |
| US8779231B2 (en) | 2010-07-07 | 2014-07-15 | Snu R&Db Foundation | Transgenic mouse for expressing human ferritin in tissue non-specific manner and use thereof |
| US10415024B2 (en) | 2012-11-16 | 2019-09-17 | Poseida Therapeutics, Inc. | Site-specific enzymes and methods of use |
| DK3310909T3 (da) | 2015-06-17 | 2021-09-13 | Poseida Therapeutics Inc | Sammensætninger og fremgangsmåder til at føre proteiner til specifikke loci i genomet |
| JP7356224B2 (ja) | 2016-03-28 | 2023-10-04 | ウルトラジェニックス ファーマシューティカル インコーポレイテッド | アデノウイルスの熱不活性化の方法 |
| WO2019126578A1 (en) | 2017-12-20 | 2019-06-27 | Poseida Therapeutics, Inc. | Compositions and methods for directing proteins to specific loci in the genome |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0300422A2 (en) * | 1987-07-21 | 1989-01-25 | The Du Pont Merck Pharmaceutical Company | An improved method for preparing stable and viable recombinant animal cell viral vectors |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1293460C (en) * | 1985-10-07 | 1991-12-24 | Brian Lee Sauer | Site-specific recombination of dna in yeast |
| JP2824434B2 (ja) * | 1989-11-28 | 1998-11-11 | 財団法人化学及血清療法研究所 | 新規発現ベクター |
| GB9123929D0 (en) * | 1991-11-11 | 1992-01-02 | Wellcome Found | Novel expression system |
| US5919676A (en) * | 1993-06-24 | 1999-07-06 | Advec, Inc. | Adenoviral vector system comprising Cre-loxP recombination |
| JP3770333B2 (ja) * | 1995-03-15 | 2006-04-26 | 大日本住友製薬株式会社 | 組換えｄｎａウイルスおよびその製造方法 |
| FR2737501B1 (fr) * | 1995-07-31 | 1997-10-24 | Transgene Sa | Nouveaux virus auxiliaires pour la preparation de vecteurs viraux recombinants |
-
1994
- 1994-09-19 JP JP25131294A patent/JP4216350B2/ja not_active Expired - Lifetime
-
1995
- 1995-08-25 AU AU30248/95A patent/AU698250B2/en not_active Expired
- 1995-08-28 CA CA002157063A patent/CA2157063C/en not_active Expired - Lifetime
- 1995-08-29 NZ NZ272883A patent/NZ272883A/en not_active IP Right Cessation
- 1995-08-30 US US08/521,575 patent/US5817492A/en not_active Expired - Lifetime
- 1995-09-13 KR KR1019950029877A patent/KR100379654B1/ko not_active IP Right Cessation
- 1995-09-14 DE DE69534902T patent/DE69534902T2/de not_active Expired - Lifetime
- 1995-09-14 AT AT95306498T patent/ATE321874T1/de not_active IP Right Cessation
- 1995-09-14 EP EP95306498A patent/EP0704534B1/en not_active Expired - Lifetime
- 1995-09-18 CN CN95116291A patent/CN1077919C/zh not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0300422A2 (en) * | 1987-07-21 | 1989-01-25 | The Du Pont Merck Pharmaceutical Company | An improved method for preparing stable and viable recombinant animal cell viral vectors |
Non-Patent Citations (2)
| Title |
|---|
| ANTON & GRAHAM (1995) J. VIROL 69(8) 4600-6 * |
| GAGE ET AL (1992) J. VIROL 66(9) 5509-15 * |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE321874T1 (de) | 2006-04-15 |
| KR960010864A (ko) | 1996-04-20 |
| KR100379654B1 (ko) | 2004-12-03 |
| CA2157063A1 (en) | 1996-03-20 |
| CA2157063C (en) | 2005-11-01 |
| EP0704534B1 (en) | 2006-03-29 |
| EP0704534A3 (en) | 1997-06-11 |
| DE69534902D1 (de) | 2006-05-18 |
| NZ272883A (en) | 1996-11-26 |
| EP0704534A2 (en) | 1996-04-03 |
| DE69534902T2 (de) | 2006-11-09 |
| US5817492A (en) | 1998-10-06 |
| JPH0884589A (ja) | 1996-04-02 |
| CN1077919C (zh) | 2002-01-16 |
| AU3024895A (en) | 1996-04-04 |
| CN1132791A (zh) | 1996-10-09 |
| JP4216350B2 (ja) | 2009-01-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU698250B2 (en) | Recombinant DNA viral vector for transfecting animal cells | |
| AU704608B2 (en) | Recombinant DNA virus and method for preparation thereof | |
| US5731172A (en) | Recombinant adenovirus and process for producing the same | |
| US7195896B2 (en) | Complementary adenoviral vector systems and cell lines | |
| EP0988389B1 (en) | Method for the production of non-group c adenoviral vectors | |
| EP0866873B1 (en) | Non-group c adenoviral vectors | |
| CA2238295C (en) | Complementary adenoviral vector systems and cell lines | |
| WO1999064582A2 (en) | High-throughput screening of gene function using libraries for functional genomics applications | |
| WO1997012986A9 (en) | Non-group c adenoviral vectors | |
| JPH10506018A (ja) | 不活化ＩＶａ２遺伝子を有する欠陥組換えアデノウィルス | |
| JP2023543291A (ja) | ＣＲＩＳＰＲ／ＣＡＳ媒介ｉｎ ｖｉｖｏ末端分離による組換えアデノウイルスのレスキュー | |
| JP2021052763A (ja) | 大きな核酸をクローニングするためのアデノウイルスベクターを作製する手段 | |
| JP4159620B2 (ja) | 組換えアデノウイルスの製造方法 | |
| JP4288259B2 (ja) | 動物細胞感染用の組換えｄｎａウイルスベクター | |
| US6740515B1 (en) | Recombinant adenovirus | |
| JP3713038B2 (ja) | 組換えアデノウイルス | |
| JPH104973A (ja) | 組換えバキュロウイルス及びその利用 | |
| AU3688399A (en) | Complementary adenoviral vector systems and cell lines |